WO1998020054A1 - Mode de fabrication de polyethylene a poids moleculaire extremement eleve et methode d'activation du support de catalyseur - Google Patents

Mode de fabrication de polyethylene a poids moleculaire extremement eleve et methode d'activation du support de catalyseur Download PDF

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Publication number
WO1998020054A1
WO1998020054A1 PCT/DE1997/002475 DE9702475W WO9820054A1 WO 1998020054 A1 WO1998020054 A1 WO 1998020054A1 DE 9702475 W DE9702475 W DE 9702475W WO 9820054 A1 WO9820054 A1 WO 9820054A1
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WO
WIPO (PCT)
Prior art keywords
mass
mol
mass loss
ppm
silica
Prior art date
Application number
PCT/DE1997/002475
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German (de)
English (en)
Inventor
Gerd Fritzsche
Heinz-Jürgen Kerrinnes
Christian Kremtz
Klaus Milowski
Original Assignee
Buna Sow Leuna Olefinverbund Gmbh
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Buna Sow Leuna Olefinverbund Gmbh filed Critical Buna Sow Leuna Olefinverbund Gmbh
Priority to CZ991622A priority Critical patent/CZ162299A3/cs
Priority to EP97945786A priority patent/EP0937107B1/fr
Priority to PL97333138A priority patent/PL333138A1/xx
Priority to DE59705706T priority patent/DE59705706D1/de
Publication of WO1998020054A1 publication Critical patent/WO1998020054A1/fr

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F10/02—Ethene
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
    • C08F210/16—Copolymers of ethene with alpha-alkenes, e.g. EP rubbers

Definitions

  • the invention relates to a method for producing ultra high molecular weight polyethylene. that works in a fluidized bed in the gas phase with a chromocene supported catalyst.
  • homopolymers and copolymers of ethylene in the density range from 0.915 to 0.955 g'cm 3 and with average molar masses of> 1 x 10 6 g / mol can be obtained in granular form, with in the gas phase in a mixed bed of small particles Polymer is carried out while removing the heat of reaction by cooling the circulating reaction gas [Ulimanns Encyklopadie der technical chemistry 4
  • ultra-high molecular weight polyethylene with a higher bulk density is produced in the presence of a mixed catalyst from an AJ organic compound with a Ti compound, which is produced by reduction of a Ti - [IV] compound, the reduction product thereafter with an Al organic compound is treated [EP 0645403; DE 4332786]
  • a highly active spherical Ziegler-Natta catalyst can be used to produce spherical polymer particles with very good flow properties and sometimes very high molecular masses with MFI (190 ° C / 5 kg) by 0.05 g / 10 min obtain the catalyst by first reacting di (organo) -Mg compounds with aluminum triethyl and 1-chloropropane to form a solid and then doping them with titanium chlorides (DE 3620060)
  • Another known process for the production of ultra-high molecular weight polyethylene with molecular weights of 1 million g / mol or greater, with densities between 0.940 to 0.950 g / cm 3 and high impact strength is characterized in that a mixture is used in mixed catalysts consisting of an alkyl aluminum component and titanium tetrachloride as alkyl aluminum component , which consists of A1R 2 X and AI (OR) RX (DE 2724096)
  • Also known is a process for the production of a catalytic system of the Ziegler type and the production of extremely high molecular weight polyethylene (1 to 3.5 million g / mol ) with this catalyst, the Ziegler-type catalyst being produced by impregnating a specific aluminum oxide with a titanium halide and then being activated with trialkyl aluminum (DE 3837524)
  • ultra-high molecular weight ethene homopolymers with molecular weights of 1.8 to 3.5 million g / mol or ethene- ⁇ -olefin copolymers with molecular weights of around 2 million g / mol can be produced by using metallocene-type compounds of titanium , Zircons or hafnium with bridged, substituted cyclopentadienyl ligands in the presence of alumoxane
  • homopolymers and copolymers of ethylene can be prepared with the following characteristic values (US 3806500. DE 2336227) Density 0, ° 45 to 0.970 g / cm 3 , melt index 0 (no flow) to 30 g / 10 min, analytically detectable content of carbon / carbon double bonds and polymer side chain branches (0.21 to 1.02 CH ⁇ / 100 C)
  • Modified, supported chromocene catalyst systems are also known, which are obtained by adding an oxidizing agent to a supported chromocene catalyst or by loading a finely divided support with an oxidizing agent and then adding chromocene and then adding a reducing agent. These can be used to polymerize olefins in the gas phase, in a suspension, in liquid monomers or in inert solvents
  • the polymers have a broad molar mass distribution and high density values.
  • An ultra-high molecular weight polyethylene with an intrinsic viscosity ⁇ of 20.6 dl / g and a density of 0.942 g / cm 3 is also available (DE 4306105)
  • the polymers obtained have MFI (190 ° C., 2.16 kg ) - Values in the range from 0.001 to 100 g / 10 min (EP 0501672)
  • Phosphate-containing oxidic supports such as silica or aluminum oxides have also been used to support chromocene in order to produce polyethylenes of a broad polymer mass spectrum using such chromocene support catalysts in slurry polymerization technology.
  • Ultra-high molecular weight ethene polymers with molecular weights of at least 3 million g / mol with a high degree of methyl branches of at least 0.4 mol% methyl branches are obtained (EP 0090374)
  • a supported catalyst which is inorganic by applying a chromium-hydrocarbon complex compound of the formula R Cr A Cr R with preferably Cvclooctetraen ligands on a finely divided, porous inorganic -oxidic carrier solid and which is optionally activated with an organoaluminum compound.
  • the polymers thus obtained have bulk densities of approximately 370 to 450 g / l and molecular weights of a very wide range up to melt indices MFI (10 ° C./21. 6 kg) from 0.5 g / 10 min to (DE 3030055)
  • the aim of the invention is to produce an ultra-high-molecular, high-tenacity polyethylene which is suitable for press sinter processing and ram extrusion, which is particularly easy to handle, by optimal mold filling, by the variability of the mold thickness and by the smoothest possible surface quality of the moldings at the same time Characterized homogeneous property level above the molded body volume
  • a process for the production of an ultra-high-molecular-weight, free-flowing polyethylene in grit form which is characterized by an optional design of the average particle size in the range> 0.42 mm at a consistently increased rubble density level, and to develop a process-specific method for catalyst carrier activation
  • the object is achieved in that in the polymerization reaction in the gas phase fluidized bed process, the velocity of the reaction gas between 0.70 m / s and 0.88 m / s, the polymerization temperature between 85 ° C and 100 ° C, the mean Minimum residence time, expressed by the ratio of polymer bed mass and the polymer mass continuously discharged from the reactor, of 3.1 h, in the reaction gas a 1-butene concentration corresponding to a partial pressure ratio Bu ⁇
  • the polymerization reaction in the gas phase fluidized bed process is preferably set so that the speed of the reactive gas is 0.74 m / s to 0.85 m / s is that a polymerization temperature is selected in the interval between 87 ° C to 95 ° C and that in the reaction cycle gas a butene-1 concentration corresponding to a partial pressure ratio of butene-1 ethene between 6 0 IC 4 mol / mol and 1 1 10 "4 mol / mol or 500 ppm to 800 ppm butene-1 and a CO 2 content between 1.5 ppm and 4.5 ppm measured
  • the separated catalyst solid is metered directly into the fluidized bed polymerization process without any thermal aging.
  • the catalyst productivity under the polymerization process conditions used according to the invention is at least 5 t polyethylene / kg catalyst solid or preferably 5.7 to 12.5 t Polyethylene / kg catalyst solid
  • the activation of the catalyst carrier is preferably carried out in such a way that the mass loss during the thermal activation of the silica is initially set to 4.1 mass% to 4.3 mass%, in this phase the mass loss speed at 38.5 ° C. to 47 5 ° C.
  • the polymer microstructure of the inventions Polvethvlene, eg the degree of polymer chain branching, can be determined both by IR spectroscopy according to JL Konig (in Spectroscopy of Polymers A.CS Professional Reference Book 1992, pages 90-91) and by NMR spectroscopy according to JC Randall (in ACS Symposium Se ⁇ es 142 (1980), page 100 and ACS-Svmposium Se ⁇ es 247 (1984. page 245)
  • the polymers according to the invention are distinguished by a gradually increased toughness behavior.
  • the measure of this is the notched impact strength (15 ° - double notch. Normal clamping bar) (DIN 63453)
  • ultra-high molecular weight polymers with viscosity numbers of up to 3000 ctr g are obtained
  • the polymers according to the invention have viscosity values of 1455 to 2450 cm 3 / g according to ISO 1 191. Shear strength values from 204 to 210 mJ / mm : according to DIN 53453 and are therefore gradually higher than known, commercially available ultra-high molecular weight PE types with 190-200 mJ / mm 2 at viscosity numbers of about 2300 cmVg In contrast to those from some known production processes, the polymers according to the invention do not contain any corrosive catalyst constituents. Accordingly, the polymers according to the invention show no corrosive effects in the processing devices
  • Examples 1-5 (Tables 1 and 2) illustrate the advantages of the process according to the invention on the basis of the characteristic properties of the polymers produced; in Example 6 the method according to the invention for activating the catalyst support is illustrated
  • amorphous silica e.g. of the type Sylopol 955 w. is activated to produce the chromocene-silica catalyst solid so that the mass loss in the thermal .
  • Activation of the silica is first set to 4.1% to 4.3% by mass that in this phase the mass loss rate at 38.5 ° C to 47.5 ° C is highest and initially no further loss of mass is to be found from 134 ° C to 136 ° C and then the mass loss is set to 0.5% by mass to 0.6% by mass with a further increase in temperature, in this phase the mass loss rate at 420 ° C is the highest to 430 ° C and that no further loss of mass occurs from 530 ° C and that the highest achievable temperature must not exceed 580 ° C.
  • the catalyst carrier silica thermally activated in this way is loaded in a conventional manner in a hydrocarbon slurry with both chromocene, so that the chromium content in the catalyst solids isolated from the hydrocarbon slurry is adjusted to 1.1% by mass of chromium.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)

Abstract

La présente invention concerne un procédé de fabrication de polyéthylène à poids moléculaire extrêmement élevé et une méthode d'activation du support de catalyseur. Les paramètres de processus relatifs au lit fluidisé en phase gazeuse ont été déterminés: temperature du réacteur, vitesse de gaz recyclé, durée effective de rétention dans le réacteur et valeurs de concentration définies de butène-1 et de CO2 dans le gaz recyclé. Elle concerne aussi une méthode d'activation thermique spéciale sur les supports de silicate d'un catalyseur à base de chromocène (la perte de masse est couplée avec la température).
PCT/DE1997/002475 1996-11-07 1997-10-24 Mode de fabrication de polyethylene a poids moleculaire extremement eleve et methode d'activation du support de catalyseur WO1998020054A1 (fr)

Priority Applications (4)

Application Number Priority Date Filing Date Title
CZ991622A CZ162299A3 (cs) 1996-11-07 1997-10-24 Způsob výroby ultravysokomolekulárního polyetylénu a metoda aktivace nosiče katalyzátoru
EP97945786A EP0937107B1 (fr) 1996-11-07 1997-10-24 Mode de fabrication de polyethylene a poids moleculaire extremement eleve et methode d'activation du support de catalyseur
PL97333138A PL333138A1 (en) 1996-11-07 1997-10-24 Method of manufacturing of ultra-large particles of polyethylene and a method of activating the catalyse carrier
DE59705706T DE59705706D1 (de) 1996-11-07 1997-10-24 Verfahren zur herstellung von ultrahochmolekularem polyethylen und methode zur aktivierung des katalysatorträgers

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19645939.7 1996-11-07
DE19645939A DE19645939A1 (de) 1996-11-07 1996-11-07 Verfahren zur Herstellung von ultrahochmolekularem Polyethylen und Methode zur Aktivierung des Katalysatorträgers

Publications (1)

Publication Number Publication Date
WO1998020054A1 true WO1998020054A1 (fr) 1998-05-14

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PCT/DE1997/002475 WO1998020054A1 (fr) 1996-11-07 1997-10-24 Mode de fabrication de polyethylene a poids moleculaire extremement eleve et methode d'activation du support de catalyseur

Country Status (9)

Country Link
US (1) US20020040113A1 (fr)
EP (1) EP0937107B1 (fr)
CZ (1) CZ162299A3 (fr)
DE (2) DE19645939A1 (fr)
ES (1) ES2170419T3 (fr)
HU (1) HUP0000107A3 (fr)
PL (1) PL333138A1 (fr)
RU (1) RU2179982C2 (fr)
WO (1) WO1998020054A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011089017A1 (fr) 2010-01-22 2011-07-28 Basell Polyolefine Gmbh Polyéthylène de poids moléculaire très élevé (uhmw)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE446980T1 (de) 2004-06-07 2009-11-15 Ticona Llc Polyethylen-pulver zur herstellung von formmassen und daraus hergestellte poröse gegenstände
JP4386923B2 (ja) * 2004-12-28 2009-12-16 旭化成ケミカルズ株式会社 超高分子量エチレン系共重合体パウダー
WO2013165983A1 (fr) 2012-05-04 2013-11-07 Ticona Llc Procédés et sorbants pour la séparation de gaz par adsorption cyclique
WO2013165996A2 (fr) 2012-05-04 2013-11-07 Ticona Llc Procédés et filtres pour le dessalement d'eau
WO2013165992A1 (fr) 2012-05-04 2013-11-07 Ticona Llc Filtration d'air en phase gazeuse
WO2015097675A2 (fr) 2013-12-23 2015-07-02 Ticona Gmbh Polyéthylène tribologiquement modifié de poids moléculaire ultra-haut
KR20180067519A (ko) 2015-09-30 2018-06-20 셀라니즈 세일즈 저머니 게엠베하 저마찰성의 스퀵 프리 어셈블리
KR102490005B1 (ko) * 2016-04-20 2023-01-19 유니베이션 테크놀로지즈, 엘엘씨 폴리머 유동 지수 조절제
WO2018032744A1 (fr) * 2016-08-19 2018-02-22 中国科学院化学研究所 Polyéthylène à ultra-haute masse moléculaire et à taille de particules ultra-fines, son procédé de préparation et son utilisation
US20190023819A1 (en) 2017-07-21 2019-01-24 Celanese Sales Germany Gmbh Conductive Ultrahigh Molecular Weight Polyethylene Compositions
US11981757B2 (en) 2019-03-25 2024-05-14 Celanese International Corporation Injection molded medical devices made from a high molecular weight polyethylene

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EP0337365A2 (fr) * 1988-04-12 1989-10-18 Union Carbide Corporation Procédé pour réduire les propriétés de gonflement d'alpha-oléfines
DD294719A5 (de) * 1990-05-28 1991-10-10 Buna Ag,De Verfahren zur herstellung von polyethylen hoher dichte
WO1994028032A1 (fr) * 1993-05-20 1994-12-08 Bp Chemicals Limited Procede de polymerisation

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GB1253063A (fr) * 1967-11-13 1971-11-10
EP0337365A2 (fr) * 1988-04-12 1989-10-18 Union Carbide Corporation Procédé pour réduire les propriétés de gonflement d'alpha-oléfines
DD294719A5 (de) * 1990-05-28 1991-10-10 Buna Ag,De Verfahren zur herstellung von polyethylen hoher dichte
WO1994028032A1 (fr) * 1993-05-20 1994-12-08 Bp Chemicals Limited Procede de polymerisation

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011089017A1 (fr) 2010-01-22 2011-07-28 Basell Polyolefine Gmbh Polyéthylène de poids moléculaire très élevé (uhmw)
US8975355B2 (en) 2010-01-22 2015-03-10 Basell Polyolefine Gmbh Ultra-high molecular weight polyethylene

Also Published As

Publication number Publication date
ES2170419T3 (es) 2002-08-01
HUP0000107A2 (hu) 2000-05-28
EP0937107B1 (fr) 2001-12-05
EP0937107A1 (fr) 1999-08-25
HUP0000107A3 (en) 2000-09-28
RU2179982C2 (ru) 2002-02-27
PL333138A1 (en) 1999-11-22
US20020040113A1 (en) 2002-04-04
DE19645939A1 (de) 1998-05-14
CZ162299A3 (cs) 1999-08-11
DE59705706D1 (de) 2002-01-17

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